Publication:
Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia

dc.contributor.buuauthorBaran, Bülent
dc.contributor.buuauthorYılmaz, Yusuf
dc.contributor.buuauthorAlgın, Oktay
dc.contributor.buuauthorKeskin, Murat
dc.contributor.buuauthorKıyıcı, Murat
dc.contributor.buuauthorKocamaz, Güzin
dc.contributor.buuauthorDolar, Enver
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentTıp Fakültesi
dc.contributor.departmentRadyoloji Ana Bilim Dalı
dc.contributor.departmentİç Hastalıkları Ana Bilim Dalı
dc.contributor.departmentGastroenteroloji Ana Bilim Dalı
dc.contributor.orcid0000-0003-4518-5283
dc.contributor.orcid0000-0001-7966-2346
dc.contributor.orcid0000-0002-3208-6211
dc.contributor.orcid0000-0002-3877-8366
dc.contributor.orcid0000-0003-4526-4352
dc.contributor.researcheridK-6651-2012
dc.contributor.researcheridAAG-9177-2021
dc.contributor.researcheridA-7978-2012
dc.contributor.scopusid35955740500
dc.contributor.scopusid22936014300
dc.contributor.scopusid23995109100
dc.contributor.scopusid23050640000
dc.contributor.scopusid6507627491
dc.contributor.scopusid23995302100
dc.contributor.scopusid6602075084
dc.date.accessioned2024-02-27T07:38:18Z
dc.date.available2024-02-27T07:38:18Z
dc.date.issued2008-04
dc.description.abstractWe report On a 43-year-old female patient with multiple thrombotic risk factors who, in a few months, developed acute myocardial infarction, an ischemic cerebrovascular event and variceal bleeding due to portal vein thrombosis. The factor V Leiden mutation was carried in heterozygous form, homocysteine was elevated at 19.6 mu mol/l, and methylene-tetrahydrofolate reductase C677T mutation was carried in. homozygous form. Moderately increased plasma homocysteine level and a reduced protein S activity were evident. Anticardiolipin IgG antibodies were mildly positive. We conclude that the presence of multiple genetic and environmental risk factors greatly amplifies the risk of clinical thrombotic events.
dc.identifier.citationBaran, B. vd. (2008). "Acute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thromblophilia". Blood Coagulation and Fibrinolysis, 19(3), 243-246.
dc.identifier.endpage246
dc.identifier.issn0957-5235
dc.identifier.issn1473-5733
dc.identifier.issue3
dc.identifier.pubmed18388507
dc.identifier.scopus2-s2.0-41849132863
dc.identifier.startpage243
dc.identifier.urihttps://doi.org/10.1097/MBC.0b013e3282f30ae5
dc.identifier.urihttps://journals.lww.com/bloodcoagulation/Fulltext/2008/04000/Acute_myocardial_infarction,_ischemic.12.aspx
dc.identifier.urihttps://hdl.handle.net/11452/39989
dc.identifier.volume19
dc.identifier.wos000255228300012
dc.indexed.scopusScopus
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherLippincott Williams & Wilkins
dc.relation.journalBlood Coagulation and Fibrinolysis
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectFactor V Leiden mutation
dc.subjectHereditary thrombophilia
dc.subjectMethylenetetrahydrofolate mutation
dc.subjectPortal vein thrombosis
dc.subjectFactor-v-leiden
dc.subjectVenous thrombosi
dc.subjectAntiphospholipid antibodies
dc.subjectCirrhotic-patients
dc.subjectRisk
dc.subjectMetaanalysis
dc.subjectDisorders
dc.subjectMutaion
dc.subjectMthfr
dc.subjectThromboembolism
dc.subjectHematology
dc.subject.emtree5,10 methylenetetrahydrofolate reductase (FADH2)
dc.subject.emtreeAcetylsalicylic acid
dc.subject.emtreeBlood clotting factor 5 Leiden
dc.subject.emtreeCardiolipin antibody
dc.subject.emtreeCarvedilol
dc.subject.emtreeClopidogrel
dc.subject.emtreeEsomeprazole
dc.subject.emtreeHomocysteine
dc.subject.emtreeImmunoglobulin G antibody
dc.subject.emtreeIsosorbide mononitrate
dc.subject.emtreeLansoprazole
dc.subject.emtreeLow molecular weight heparin
dc.subject.emtreeNadroparin
dc.subject.emtreePravastatin
dc.subject.emtreeProtein S
dc.subject.emtreeProton pump inhibitor
dc.subject.emtreeAcute heart infarction
dc.subject.emtreeAdult
dc.subject.emtreeArticle
dc.subject.emtreeBleeding
dc.subject.emtreeCase report
dc.subject.emtreeCerebrovascular accident
dc.subject.emtreeCoronary stent
dc.subject.emtreeDrug substitution
dc.subject.emtreeDrug withdrawal
dc.subject.emtreeEnvironmental factor
dc.subject.emtreeFemale
dc.subject.emtreeGene mutation
dc.subject.emtreeGenetic risk
dc.subject.emtreeHeterozygosity
dc.subject.emtreeHomozygosity
dc.subject.emtreeHuman
dc.subject.emtreePercutaneous coronary intervention
dc.subject.emtreePortal vein thrombosis
dc.subject.emtreePortal vein thrombosis
dc.subject.emtreeProtein function
dc.subject.emtreeRisk factor
dc.subject.emtreeThrombophilia
dc.subject.emtreeThrombosis
dc.subject.emtreeUpper gastrointestinal bleeding
dc.subject.emtreeVarix bleeding
dc.subject.meshAdult
dc.subject.meshFactor V
dc.subject.meshFemale
dc.subject.meshGenetic predisposition to disease
dc.subject.meshHumans
dc.subject.meshMethylenetetrahydrofolate reductase (nadph2)
dc.subject.meshMyocardial infarction
dc.subject.meshPortal vein
dc.subject.meshStroke
dc.subject.meshThrombophilia
dc.subject.meshVenous thrombosis
dc.subject.scopusMutation; Prothrombin; Activated Protein C Resistance
dc.subject.wosHematology
dc.titleAcute myocardial infarction, ischemic cerebrovascular disease and variceal bleeding due to portal vein thrombosis in a patient with hereditary thrombophilia
dc.typeArticle
dc.wos.quartileQ4
dspace.entity.typePublication
local.contributor.departmentTıp Fakültesi/İç Hastalıkları Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Radyoloji Ana Bilim Dalı
local.contributor.departmentTıp Fakültesi/Gastroenteroloji Ana Bilim Dalı
local.indexed.atWOS
local.indexed.atScopus

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